Carl Zeiss Meditec AG: Medical Device Recall in 2021 - (Recall #: Z-1133-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

IOLMaster 700

Product Classification:

Class II

Date Initiated: December 7, 2020

Date Posted: February 24, 2021

Recall Number: Z-1133-2021

Event ID: 87055

Reason for Recall:

When using software 1.90.2.09 or 1.90.8.06 and using modality worklist functionality for patient data transfer, the selection of the patient in the patient list may not match the patient information displayed on the right side of the screen

Status: Terminated

Product Quantity: 613 devices

Code Information:

Model: IOLMaster 700 Catalog Number device: 000000-1932-169

Distribution Pattern:

U.S.: AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, LA, MA, MD, ME, MI, MO, MS, NC, NE, NH, NJ, NM, NV, NY, OH, OK, PA, Puerto Rico, SC, TX, UT, VA, VT, WA, WI, and WV. O.U.S.: Austria, Australia, Canada, Switzerland, Czech Republic, Germany, Denmark, Estonia, Spain, France, United Kingdom, Guatemala, Hong Kong, Indonesia, Ireland, India, Italy, Japan, Kuwait, Malaysia, Netherlands, New Zealand, Philippines, Poland, Portugal, Russia, Sweden, Singapore, Slovakia, Thailand, Taiwan, and South Africa.

Voluntary or Mandated:

Voluntary: Firm initiated